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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047284inversion1nstd229human GRCh38 chr5: 18,365,039-24,500,882 , GRCh37.p13 chr5: 18,365,148-24,500,991 LOC105374683, SNORA105A, 40 more genes
    nsv7047140inversion1nstd229human GRCh38 chr5: 21,512,061-29,406,624 , GRCh37.p13 chr5: 21,512,170-29,406,731 AKTIPP2, RNU4-43P, 48 more genes
    nsv7045172inversion1nstd229human GRCh38 chr5: 18,376,939-24,500,874 , GRCh37.p13 chr5: 18,377,048-24,500,983 LOC102723561, LOC100420804, 40 more genes
    nsv6772781copy number variation1nstd229human GRCh38 chr5: 24,044,092-24,235,656 , GRCh37.p13 chr5: 24,044,201-24,235,765 LOC503540, LINC02899, 1 more genes
    nsv6765519copy number variation1nstd229human GRCh38 chr5: 23,861,039-24,222,026 , GRCh37.p13 chr5: 23,861,148-24,222,135 AKTIPP2, LINC02899, 1 more genes
    nsv6761826copy number variation1nstd229human GRCh38 chr5: 24,152,001-24,183,700 , GRCh37.p13 chr5: 24,152,110-24,183,809 AKTIPP2, LINC02899, 1 more genes
    nsv6760245copy number variation1nstd229human GRCh38 chr5: 24,154,066-24,176,537 , GRCh37.p13 chr5: 24,154,175-24,176,646 AKTIPP2, LOC503540, 1 more genes
    nsv6758719copy number variation1nstd229human GRCh38 chr5: 18,040,306-26,567,940 , GRCh37.p13 chr5: 18,040,415-26,568,049 CDH12, LINC02899, 49 more genes
    nsv6758397copy number variation1nstd229human GRCh38 chr5: 23,793,608-24,196,145 , GRCh37.p13 chr5: 23,793,717-24,196,254 LINC02899, LOC503540, 2 more genes
    nsv6758102copy number variation1nstd229human GRCh38 chr5: 22,276,907-24,693,876 , GRCh37.p13 chr5: 22,277,016-24,693,985 LINC02899, LOC105374686, 14 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6394734copy number variation1nstd223human GRCh38 chr5: 24,044,092-24,235,652 , GRCh37.p13 chr5: 24,044,201-24,235,761 AKTIPP2, LINC02899, 1 more genes
    nsv6379595copy number variation1nstd223human GRCh38 chr5: 23,793,607-24,196,144 , GRCh37.p13 chr5: 23,793,716-24,196,253 LOC503540, LINC02899, 2 more genes
    nsv6377048copy number variation1nstd223human GRCh38 chr5: 24,172,701-24,173,900 , GRCh37.p13 chr5: 24,172,810-24,174,009 LINC02899, LOC503540
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 more genes
    nsv6136143copy number variation1nstd213human GRCh37 chr5: 9,360,000-26,560,001 , GRCh38.p12 chr5: 9,359,888-26,559,892 FTH1P10, MYO10, 163 more genes
    nsv6136107copy number variation1nstd213human GRCh37 chr5: 22,320,000-25,100,001 , GRCh38.p12 chr5: 22,319,891-25,099,892 CDH10, LOC503540, 17 more genes
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